| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ITGA7, LOC126861535 (A362P +13 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | ITGA7, LOC126861535 (T313A +13 more) | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency +1 more | |
| | ITGA7, LOC126861535 (S696L +12 more) | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency +2 more | |
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